Biochemistry
10 questionsIn which condition does serum appear milky white?
Which amino acid among the following has significant UV absorption at 280 nm used in protein quantification?
In starvation, nitrogen is primarily carried from muscle to liver and kidney by which amino acid?
Chemiosmotic coupling of oxidative phosphorylation is related to which of the following?
What is the coenzyme form of pyridoxine?
What is the function of primase?
Which RNA is used in RNA splicing?
Which of the following enzymes is not involved in the urea cycle?
Which of the following GAG is not sulfated?
Which of the following is a true difference between gangliosides and cerebrosides?
NEET-PG 2012 - Biochemistry NEET-PG Practice Questions and MCQs
Question 71: In which condition does serum appear milky white?
- A. Increased LDL
- B. Increased HDL
- C. Increased VLDL
- D. Increased Chylomicrons (Correct Answer)
Explanation: ***Increased Chylomicrons*** - **Chylomicrons** are the largest lipoprotein particles (75-1200 nm) with the highest **triglyceride content (85-95%)**, giving serum a characteristic **milky white** or "creamy" appearance - This intense milky appearance occurs after **fatty meals** (postprandial lipemia) or in **Type I and V hyperlipidemias** (familial chylomicronemia syndrome) - The **light scattering** by these large particles makes the serum completely opaque, distinguishing it from other lipid abnormalities - Classic clinical finding: **"cream layer" forms on top** when lipemic serum stands overnight in refrigerator *Increased LDL* - Elevated **Low-Density Lipoprotein (LDL)** produces **clear to slightly hazy** serum, never milky white - LDL particles are much smaller (18-25 nm) than chylomicrons and contain primarily **cholesterol**, not triglycerides - High LDL is a cardiovascular risk factor but does not cause visible lipemia *Increased HDL* - **High-Density Lipoprotein (HDL)** elevation results in **clear serum** - HDL particles are the smallest (5-12 nm) and densest lipoproteins - High HDL is protective and causes no turbidity *Increased VLDL* - **Very Low-Density Lipoprotein (VLDL)** elevation can cause **turbid or hazy** serum in severe hypertriglyceridemia, but typically less intensely milky than chylomicrons - VLDL particles are smaller (30-80 nm) than chylomicrons with lower triglyceride content (50-65%) - In Type IV hyperlipidemia (isolated VLDL elevation), serum appears uniformly turbid without cream layer formation - The most dramatic "milky white" appearance is specifically associated with **chylomicronemia**
Question 72: Which amino acid among the following has significant UV absorption at 280 nm used in protein quantification?
- A. Tyrosine (Correct Answer)
- B. Alanine
- C. Histidine
- D. Arginine
Explanation: ***Correct Option: Tyrosine*** - Tyrosine contains a **phenol functional group** (aromatic ring with hydroxyl group), giving it **significant UV absorption at 280 nm** (specifically ~274 nm) - Along with **tryptophan** and **phenylalanine**, tyrosine is one of the three aromatic amino acids used for **protein quantification via UV spectroscopy** - The aromatic side chain with conjugated double bonds enables strong UV light absorption *Incorrect Option: Alanine* - Alanine has a **methyl group** as its side chain (non-polar, aliphatic) - **Lacks aromatic rings** or conjugated systems - Does **not absorb UV light** at 280 nm *Incorrect Option: Histidine* - Histidine has an **imidazole ring** (heterocyclic aromatic) in its side chain - While technically aromatic, it has **minimal UV absorption at 280 nm** (weak absorption around 210-230 nm) - **Not used for protein quantification** at 280 nm due to insignificant absorption at this wavelength *Incorrect Option: Arginine* - Arginine contains a **guanidinium group** (highly basic, polar) - **Non-aromatic structure** without conjugated double bonds - Does **not exhibit UV absorption** at wavelengths used for protein analysis
Question 73: In starvation, nitrogen is primarily carried from muscle to liver and kidney by which amino acid?
- A. Alanine (Correct Answer)
- B. Glycine
- C. Aspartic acid
- D. Asparagine
Explanation: ***Alanine*** - During starvation, muscles break down proteins, and the amino groups from these proteins are transferred to **pyruvate** to form **alanine** via the **glucose-alanine cycle (Cahill cycle)**. - **Alanine** is then released into the bloodstream and transported primarily to the **liver**, where its carbon skeleton can be used for **gluconeogenesis** and the amino group enters the urea cycle. - Note: While alanine is the primary carrier to the liver, **glutamine** is the main nitrogen carrier to the kidney. However, among the given options, alanine is unequivocally the correct answer. *Aspartic acid* - While aspartate is involved in amino group transfer and is a crucial component of the **urea cycle**, it is not the primary carrier for inter-organ nitrogen transport from muscle to liver during starvation. - Its role is more localized within the liver for the urea cycle rather than as a transport amino acid. *Glycine* - Glycine plays roles in various metabolic pathways, including synthesis of heme, purines, and conjugation reactions, but it is not the primary amino acid for carrying nitrogen from muscle to liver during starvation. - Its small size and simple structure make it less suitable for efficient nitrogen transport compared to alanine. *Asparagine* - Asparagine has a minor role in nitrogen transport but is not the primary carrier during starvation. - It is synthesized from **aspartate** and ammonia and is typically involved in protein synthesis and nitrogen storage in some tissues.
Question 74: Chemiosmotic coupling of oxidative phosphorylation is related to which of the following?
- A. ATP generation by pumping of neutrons
- B. Formation of ATP at substrate level
- C. ATP generation by pumping of protons (Correct Answer)
- D. ATP formation by transport of electrons
Explanation: ***ATP generation by pumping of protons*** - **Chemiosmotic coupling** links the electron transport chain's activity to ATP synthesis through the generation of a **proton gradient** across the inner mitochondrial membrane. - The energy released from the flow of electrons through complexes I, III, and IV is used to pump protons from the mitochondrial matrix to the intermembrane space, creating a **proton motive force** that drives ATP synthase. *Formation of ATP at substrate level* - **Substrate-level phosphorylation** involves the direct transfer of a phosphate group from a high-energy substrate to ADP to form ATP, independently of a proton gradient. - This process occurs in reactions like those in **glycolysis** and the **Krebs cycle**, not in oxidative phosphorylation via chemiosmosis. *ATP generation by pumping of neutrons* - **Neutrons** are subatomic particles with no electric charge and are not involved in biological processes like ATP generation or membrane transport. - Pumping of neutrons has no physiological relevance in cellular energy metabolism. *ATP formation by transport of electrons* - While **electron transport** is an integral part of oxidative phosphorylation, it does not directly form ATP. - The energy released during electron transport is used to create the **proton gradient** (chemiosmotic coupling), which then drives ATP synthesis, rather than ATP being formed directly by electron movement.
Question 75: What is the coenzyme form of pyridoxine?
- A. ADP
- B. NAD
- C. PLP (Correct Answer)
- D. FAD
Explanation: ***PLP*** - **Pyridoxal phosphate (PLP)** is the active coenzyme form of **pyridoxine (vitamin B6)**. - It plays a crucial role in numerous metabolic reactions, particularly those involving **amino acid metabolism**. *ADP* - **Adenosine diphosphate (ADP)** is an important molecule in energy transfer, particularly in the formation of **ATP (adenosine triphosphate)**. - It is not a coenzyme form of any vitamin, but rather a **nucleotide**. *NAD* - **Nicotinamide adenine dinucleotide (NAD)** is a coenzyme derived from **niacin (vitamin B3)**. - It functions as an electron carrier in **redox reactions** and is vital for cellular respiration. *FAD* - **Flavin adenine dinucleotide (FAD)** is a coenzyme derived from **riboflavin (vitamin B2)**. - It also serves as an electron carrier in **redox reactions**, particularly in the electron transport chain.
Question 76: What is the function of primase?
- A. Joining DNA fragments
- B. Synthesizing small RNA fragments during translation
- C. Unwinding of DNA
- D. Synthesizing small RNA fragments during DNA synthesis (Correct Answer)
Explanation: ***Synthesizing small RNA fragments during DNA synthesis*** - **Primase** is an enzyme that synthesises short **RNA primers** which are crucial for initiating DNA replication. - These **RNA primers** provide a free 3'-hydroxyl group, which **DNA polymerase** requires to start adding deoxyribonucleotides. *Joining DNA fragments* - This function is primarily carried out by **DNA ligase**, which forms phosphodiester bonds between adjacent nucleotides to join DNA fragments. - **DNA ligase** is essential for repairing DNA breaks and joining **Okazaki fragments** on the lagging strand during replication. *Synthesising small RNA fragments during translation* - Small RNA fragments are generally involved in **gene regulation** (e.g., microRNAs) or structural components of ribosomes (e.g., ribosomal RNA) during translation, but primase is not involved in their synthesis for this purpose. - The synthesis of **mRNA**, **tRNA**, and **rRNA** during translation is carried out by **RNA polymerases**, not **primase**. *Unwinding of DNA* - The **unwinding of the DNA double helix** is primarily performed by an enzyme called **DNA helicase**. - **DNA helicase** breaks the hydrogen bonds between complementary base pairs, separating the two strands to allow replication or transcription to proceed.
Question 77: Which RNA is used in RNA splicing?
- A. mRNA
- B. tRNA
- C. rRNA
- D. Small nuclear RNA (snRNA) (Correct Answer)
Explanation: ***Small nuclear RNA (snRNA)*** - **snRNAs** are key components of **spliceosomes**, the molecular machines that catalyze the removal of introns from pre-mRNA. - They bind to specific sequences within the pre-mRNA and facilitate the splicing reactions. *mRNA* - **mRNA (messenger RNA)** carries the genetic code from DNA to the ribosomes for **protein synthesis**. - While it is the molecule that gets spliced, it does not directly participate in the splicing machinery itself. *rRNA* - **rRNA (ribosomal RNA)** is a structural and catalytic component of **ribosomes**, where protein synthesis occurs. - It plays no direct role in the process of RNA splicing. *tRNA* - **tRNA (transfer RNA)** molecules are responsible for carrying specific **amino acids** to the ribosome during protein synthesis. - They are involved in translation, not in the processing of RNA by splicing.
Question 78: Which of the following enzymes is not involved in the urea cycle?
- A. Arginase
- B. Argininosuccinate lyase
- C. CPS-II (Correct Answer)
- D. CPS-I
Explanation: ***CPS-II*** - Carbamoyl phosphate synthetase II is involved in **pyrimidine synthesis**, not the urea cycle. - It uses **glutamine** as a nitrogen donor and is located in the **cytosol**. *CPS-I* - Carbamoyl phosphate synthetase I is the **rate-limiting enzyme** of the urea cycle. - It catalyzes the formation of **carbamoyl phosphate** from **ammonia**, CO2, and ATP in the mitochondria. *Arginase* - Arginase is the **final enzyme** in the urea cycle, converting **arginine** to **ornithine** and **urea**. - This reaction occurs in the cytosol and releases urea for excretion. *Argininosuccinate lyase* - Argininosuccinate lyase catalyzes the cleavage of **argininosuccinate** into **fumarate** and **arginine**. - This is a key step in regenerating arginine for the final step of the urea cycle.
Question 79: Which of the following GAG is not sulfated?
- A. Keratan sulfate
- B. Dermatan sulfate
- C. Chondroitin sulfate
- D. Hyaluronic acid (Correct Answer)
Explanation: ***Hyaluronic acid*** - **Hyaluronic acid** is unique among glycosaminoglycans (GAGs) because it is the only one that is **not sulfated**. - It also distinguishes itself by being the only GAG that does **not form proteoglycans** and is not synthesized in the Golgi apparatus. *Chondroitin sulfate* - **Chondroitin sulfate** is a sulfated glycosaminoglycan that is a major component of the **extracellular matrix**, particularly in cartilage. - Its sulfate groups contribute to its **negative charge**, allowing it to attract water and provide resistance to compression. *Dermatan sulfate* - **Dermatan sulfate** is another sulfated GAG, found predominantly in the skin, blood vessels, and heart valves. - It contains **sulfate groups**, which are crucial for its interactions with various proteins and its role in tissue structure. *Keratan sulfate* - **Keratan sulfate** is a sulfated GAG found in the cornea, cartilage, and bone. - It is distinct from other GAGs due to its **lack of uronic acid** and the presence of sulfate groups.
Question 80: Which of the following is a true difference between gangliosides and cerebrosides?
- A. Specific carbohydrate composition
- B. Charge difference (Correct Answer)
- C. Location in the nervous system
- D. Presence of glucose
Explanation: ***Charge difference*** - **Gangliosides** contain **sialic acid (N-acetylneuraminic acid)** residues, which are negatively charged, making gangliosides **anionic**. - **Cerebrosides** are **neutral glycosphingolipids** as they lack charged sugar residues. *Specific carbohydrate composition* - While both have carbohydrate components, referring to "specific carbohydrate composition" as the *true difference* is too broad. Both have characteristic sugar groups, but the **presence of sialic acid** in gangliosides is the key differentiator in charge. - Cerebrosides typically contain a single sugar (either glucose or galactose), whereas gangliosides have a more complex oligosaccharide chain including sialic acid. *Presence of glucose* - Both cerebrosides (specifically **glucocerebrosides**) and gangliosides can contain **glucose** in their carbohydrate moieties. - This is not a distinguishing feature; the *type* and *arrangement* of sugars, particularly the presence of sialic acid, are more specific. *Location in the nervous system* - Both gangliosides and cerebrosides are abundant in the **nervous system**, particularly in cell membranes. - Their presence in the nervous system is a similarity, not a differentiating factor.